Department of Medicine, Federal University of Sao Joao del-Rei, Divinopolis, Minas Gerais 35501-296, Brazil.
Department of Pediatric Oncology, Federal University of Sao Paulo, Sao Paulo, Sao Paulo 04021-001, Brazil.
Clin Genitourin Cancer. 2024 Oct;22(5):102154. doi: 10.1016/j.clgc.2024.102154. Epub 2024 Jul 11.
Platinum-based chemotherapy (CTX) has historically been the primary treatment for advanced urothelial cancer (aUC), with limited alternative options. The therapeutic landscape experienced a paradigm shift following the results of the EV-302 and Checkmate-901 trials, which led to the approval of Enfortumab vedotin plus pembrolizumab (EV-P) as the preferred first-line treatment, and nivolumab plus CTX for those unable to receive the preferred regimen. Currently, further investigations are underway to explore PD-1 and PD-L1 inhibitors in the initial treatment of aUC.
We conducted a systematic search across PubMed, Embase, and the Cochrane Library for randomized controlled trials (RCTs) comparing immune checkpoint inhibitors (ICI)-CTX combinations versus CTX alone as first-line treatment for advanced UC. Employing a random-effects model, we pooled hazard ratios (HR) with 95% confidence intervals (CI).
Our analysis encompassed 3 RCTs, involving 2162 participants, with 51.16% randomized to combination therapy with platinum-based CTX. Compared to CTX alone, immune-chemotherapy significantly improved overall survival (HR 0.84; 95% CI 0.75-0.93; P < .01), progression-free survival (HR 0.78; 95% CI 0.70-0.86; P < .01), and objective response rate (RR 1.20; 95% CI 1.06-1.36; P < .01), while elevating the risk of immune-related adverse events (P-value = .02).
In this meta-analysis of RCTs, ICI plus CTX demonstrated a significant association with improved survival at the expense of an increased risk of immune-related adverse events. Therefore, our findings suggest that this combination should be considered as an initial treatment for aUC in platinum-eligible patients who cannot receive EV-P.
铂类化疗(CTX)一直以来都是治疗晚期尿路上皮癌(aUC)的主要手段,可选方案有限。EV-302 和 Checkmate-901 试验的结果带来了治疗模式的重大转变,使 Enfortumab vedotin 联合 pembrolizumab(EV-P)成为首选一线治疗方案,对于不能接受首选方案的患者则采用nivolumab 联合 CTX。目前,正在进行进一步的研究,以探索 PD-1 和 PD-L1 抑制剂在 aUC 的初始治疗中的应用。
我们在 PubMed、Embase 和 Cochrane 图书馆中进行了系统检索,以查找比较免疫检查点抑制剂(ICI)-CTX 联合治疗与 CTX 单药作为晚期 UC 一线治疗的随机对照试验(RCT)。我们采用随机效应模型,汇总危险比(HR)及其 95%置信区间(CI)。
我们的分析纳入了 3 项 RCT,共纳入 2162 名参与者,其中 51.16%随机分配至铂类 CTX 联合免疫治疗组。与 CTX 单药治疗相比,免疫化疗显著改善了总生存期(HR 0.84;95%CI 0.75-0.93;P<.01)、无进展生存期(HR 0.78;95%CI 0.70-0.86;P<.01)和客观缓解率(RR 1.20;95%CI 1.06-1.36;P<.01),同时增加了免疫相关不良事件的风险(P 值=0.02)。
在这项 RCT 的荟萃分析中,ICI 联合 CTX 显示与生存改善显著相关,但增加了免疫相关不良事件的风险。因此,我们的研究结果表明,对于不能接受 EV-P 的铂类治疗有效的 aUC 患者,该联合方案应考虑作为初始治疗方案。